Canonical Allele Identifier: CA362185134
Gene: GABRG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162103966C>G , CM000667.2:g.162103966C>G GRCh38
NC_000005.9:g.161530972C>G , CM000667.1:g.161530972C>G GRCh37
NC_000005.8:g.161463550C>G NCBI36
NG_009290.1:g.41325C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000356592.8:c.671C>G
ENST00000361925.9:c.829C>G ENSP00000354651.5:p.Leu277Val
ENST00000522053.2:n.600C>G
ENST00000523372.2:c.792C>G
ENST00000638552.1:c.424C>G ENSP00000491763.1:p.Leu142Val
ENST00000638660.1:c.424C>G ENSP00000492869.1:p.Leu142Val
ENST00000638772.1:c.709C>G ENSP00000491557.1:p.Leu237Val
ENST00000638782.1:n.771C>G
ENST00000638877.1:c.586C>G
ENST00000639046.1:c.100C>G ENSP00000492659.1:p.Leu34Val
ENST00000639111.2:c.709C>G ENSP00000492125.2:p.Leu237Val
ENST00000639213.2:c.709C>G MANE Select ENSP00000491909.2:p.Leu237Val
ENST00000639278.1:c.637C>G ENSP00000491958.1:p.Leu213Val
ENST00000639384.1:c.709C>G ENSP00000491240.1:p.Leu237Val
ENST00000639424.1:c.107+35860C>G ENSP00000491245.1:n.107+35860C>G
ENST00000639683.1:c.643C>G ENSP00000492581.1:p.Leu215Val
ENST00000639975.1:c.643C>G ENSP00000492096.1:p.Leu215Val
ENST00000640574.1:c.424C>G ENSP00000491582.1:p.Leu142Val
ENST00000640739.1:n.3240C>G
ENST00000640910.1:c.147C>G
ENST00000640985.1:c.622C>G ENSP00000492293.1:p.Leu208Val
ENST00000641017.1:c.709C>G ENSP00000493461.1:p.Leu237Val
ENST00000356592.7:c.709C>G ENSP00000349000.3:p.Leu237Val
ENST00000361925.8:c.709C>G ENSP00000354651.4:p.Leu237Val
ENST00000414552.6:c.829C>G ENSP00000410732.2:p.Leu277Val
ENST00000522053.1:c.424C>G ENSP00000430182.1:p.Leu142Val
ENST00000522990.5:c.*311C>G ENSP00000430732.1:n.*311C>G
ENST00000523372.1:c.830C>G ENSP00000430124.1:n.830C>G
NM_000816.3:c.709C>G NP_000807.2:p.Leu237Val
NM_198903.2:c.829C>G NP_944493.2:p.Leu277Val
NM_198904.2:c.709C>G NP_944494.1:p.Leu237Val
NM_001375339.1:c.700C>G NP_001362268.1:p.Leu234Val
NM_001375340.1:c.709C>G NP_001362269.1:p.Leu237Val
NM_001375341.1:c.709C>G NP_001362270.1:p.Leu237Val
NM_001375342.1:c.709C>G NP_001362271.1:p.Leu237Val
NM_001375343.1:c.829C>G NP_001362272.1:p.Leu277Val
NM_001375344.1:c.709C>G NP_001362273.1:p.Leu237Val
NM_001375345.1:c.643C>G NP_001362274.1:p.Leu215Val
NM_001375346.1:c.643C>G NP_001362275.1:p.Leu215Val
NM_001375347.1:c.622C>G NP_001362276.1:p.Leu208Val
NM_001375348.1:c.289C>G NP_001362277.1:p.Leu97Val
NM_001375349.1:c.424C>G NP_001362278.1:p.Leu142Val
NM_001375350.1:c.289C>G NP_001362279.1:p.Leu97Val
NM_198904.3:c.709C>G NP_944494.1:p.Leu237Val
NM_198904.4:c.709C>G MANE Select NP_944494.1:p.Leu237Val